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  Remote control of neuronal activity with a light-gated glutamate receptor

Szobota, S., Gorostiza, P., Del Bene, F., Wyart, C., Fortin, D. L., Kolstad, K. D., et al. (2007). Remote control of neuronal activity with a light-gated glutamate receptor. Neuron, 54(4), 535-545. doi:10.1016/j.neuron.2007.05.010.

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Szobota, S., Autor
Gorostiza, P., Autor
Del Bene, F., Autor
Wyart, C., Autor
Fortin, D. L., Autor
Kolstad, K. D., Autor
Tulyathan, O., Autor
Volgraf, M., Autor
Numano, R., Autor
Aaron, H. L., Autor
Scott, E. K., Autor
Kramer, R. H., Autor
Flannery, J., Autor
Baier, Herwig1, Autor           
Trauner, D., Autor
Isacoff, E. Y., Autor
Affiliations:
1University of California, San Francisco, U.S.A., ou_persistent22              

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Schlagwörter: neural circuitry induced activation visual responses transgenic mice excitable cells optical control bound agonists ion channels in-vivo zebrafish Neurosciences & Neurology
 Zusammenfassung: The ability to stimulate select neurons in isolated tissue and in living animals is important for investigating their role in circuits and behavior. We show that the engineered light-gated ionotropic glutamate receptor (LiGluR), when introduced into neurons, enables remote control of their activity. Trains of action potentials are optimally evoked and extinguished by 380 nm and 500 nm light, respectively, while intermediate wavelengths provide graded control over the amplitude of depolarization. Light pulses of 1-5 ms in duration at similar to 380 nm trigger precisely timed action potentials and EPSP-like responses or can evoke sustained depolarizations that persist for minutes in the dark until extinguished by a short pulse of similar to 500 nm light. When introduced into sensory neurons in zebrafish larvae, activation of LiGluR reversibly blocks the escape response to touch. Our studies show that LiGluR provides robust control over neuronal activity, enabling the dissection and manipulation of neural circuitry in vivo.

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Sprache(n): eng - English
 Datum: 2007
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: Anderer: WOS:000246970800009
DOI: 10.1016/j.neuron.2007.05.010
ISSN: 0896-6273
 Art des Abschluß: -

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Titel: Neuron
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: Cambridge, Mass. : Cell Press
Seiten: - Band / Heft: 54 (4) Artikelnummer: - Start- / Endseite: 535 - 545 Identifikator: ISSN: 0896-6273
CoNE: https://pure.mpg.de/cone/journals/resource/954925560565